3,6-BIS(TRIPHENYLPHOSPHONIUM)-CYCLOHEXENE PEROXODISULFATE: A HIGHLY EFFICIENT OXIDANT FOR THE SELECTIVE OXIDATION OF BENZYLIC ALCOHOLS
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1081/SCC-100106207
Reference19 articles.
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4. Fenton's reagent. V. Hydroxylation and side-chain cleavage of aromatics
5. Benzyltriphenylphosphonium Peroxodisulfate (PhCH2PPh3)2S2O8: a Mild and Inexpensive Reagent for Efficient Oxidation of Organic Compounds under Nonaqueous and Aprotic Conditions
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1. Synthesis, crystal structure, Hirshfeld surface analysis, DFT calculations and characterization of 1,3-propanediylbis(triphenylphosphonium) monotribromide as brominating agent of double bonds and phenolic rings;Journal of Molecular Structure;2020-04
2. Formation of Aldehydes and Ketones by Oxidation;Comprehensive Organic Transformations;2018-02-28
3. ChemInform Abstract: 3,6-Bis(triphenylphosphonium)cyclohexene Peroxodisulfate: A Highly Efficient Oxidant for the Selective Oxidation of Benzylic Alcohols.;ChemInform;2010-05-23
4. Sulfur and Phosphorus Peroxides;PATAI'S Chemistry of Functional Groups;2009-12-15
5. 1,4-Bis(triphenylphosphonium)-2-butene Peroxodisulfate: An Efficient Reagent for Synthesis of β-Nitrato Alcohols;Synthetic Communications;2009-11-05
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